Laurent Villard

Mutations in a putative global transcriptional regulator cause X-linked mental retardation with α-thalassemia (ATR-X syndrome)

Richard J. Gibbons, David J. Picketts, Laurent Villard et al. · Cell · 1995 · 632 citations · Full text

Life Sciences, Genetics, Molecular Genetics +6

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

Markus Wolff, Katrine M. Johannesen, Ulrike B. S. Hedrich et al. · Brain · 2017 · 575 citations · Full text

Medicine, Genetics, Neurology +17

Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes

Sabine Endele, Georg Rosenberger, Kirsten Geider et al. · Nature Genetics · 2010 · 509 citations

Life Sciences, Genetics, Neuroscience +16

Mecp2 Deficiency Disrupts Norepinephrine and Respiratory Systems in Mice

Jean‐Charles Viemari, Jean‐Christophe Roux, Andrew K. Tryba et al. · Journal of Neuroscience · 2005 · 288 citations · Full text

Life Sciences, Genetics, Neuroscience +16

Two affected boys in a Rett syndrome family

Laurent Villard, Arlette Kpebe, Carlos Cardoso et al. · Neurology · 2000 · 195 citations

Life Sciences, Genetics, Molecular Genetics +14